DNA cleavage reactions by type II restriction enzymes that require two copies of their recognition sites

Several type II restriction endonucleases interact with two copies of their target sequence before they cleave DNA. Three such enzymes, NgoMIV, Cfr10I and NaeI, were tested on plasmids with one or two copies of their recognit ion sites, and on catenanes containing two interlinked rings of DNA with on e site in each ring. The enzymes showed distinct patterns of behaviour. Ngo MIV and NaeI cleaved the plasmid with two sites faster than that with one s ite and the catenanes at an intermediate rate, while Cfr10I gave similar st eady-state rates on all three substrates. Both Cfr10I and NgoMIV converted the majority of the substrates with two sites directly to the products cut at both sites, while NaeI cleaved just one site at a time. All three enzyme s thus synapse two DNA sites through three-dimensional space before cleavin g DNA. With Cfr10I and NgoMIV, both sites are cleaved in one turnover, in a manner consistent with their tetrameric structures, while the cleavage of a single site by NaeI indicates that the second site acts not as a substrat e but as an activator, as reported previously. The complexes spanning two s ites have longer lifetimes on catenanes with one site in each ring than on circular DNA with two sites, which indicates that the catenanes have more f reedom for site juxtaposition than plasmids with sites in cis. (C) 2001 Aca demic Press.